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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857802Generated: November 1, 2026

3-(3,5-Bis(trifluoromethyl)benzylamino)propanol → N-[3,5-Bis(trifluoromethyl)benzyl]-2-chloro-N-(3-hydroxypropyl)-6-methyl-4-phenyl-3-pyridinecarboxamide

https://huagongshe.com/reaction/1857802

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3,5-Bis(trifluoromethyl)benzylamino)propanolHCID 11638019—
Reactant2-Chloro-6-methyl-4-phenyl-3-pyridinecarboxylic acidHCID 18387271—
Reactant2-Chloro-4-phenylnicotinic acidHCID 18387312—
ReactantN-[3,5-bis(trifluoromethyl)benzyl]-N-(2-hydroxyethyl)amineHCID 22248766—
ProductN-[3,5-Bis(trifluoromethyl)benzyl]-2-chloro-N-(3-hydroxypropyl)-6-methyl-4-phenyl-3-pyridinecarboxamideHCID 18387316—

Reaction Steps

The same process as in Step 2 in Reference Example 12 was repeated, except that 2-chloro-6-methyl-4-phenyl-3-pyridinecarboxylic acid was reacted with N-[3,5-bis(trifluoromethyl)benzyl]-N-(3-hydroxypropyl)amine in place of reacting 2-chloro-4-phenyl-3-pyridinecarboxylic acid with N-[3,5-bis(trifluoromethyl)benzyl]-N-(2-hydroxyethyl)amine, to obtain the entitled compound as a pale-yellow, oily substance. NMR(200 MHz, CDCl3) ppm: 1.15-1.65(2H,m), 2.59(3H,s), 2.75-3.20(2H,m), 4.06(1H×2/5,d,J=15.4 Hz), 4.31(1H×2/5,d,J=15.4 Hz), 4.65(1H×3/5,d,J=15.2 Hz), 4.74(1H×3/5,d,J=15.2 Hz), 7.16(1H,s), 7.20-7.60(5H,m), 7.72(2H,s), 7.78(1H,s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147071
Source datasetuspto-grants-2000_11
ORD IDord-94368747ed8c4efb8447a587d1b39dcc
Source noteuspto-grants-2000_11